Vesin M F, Barakat-Walter I, Droz B
Institut d'Histologie et d'Embryologie, Faculté de Médecine, Université de Lausanne, Switzerland.
J Neurochem. 1991 Jul;57(1):167-74. doi: 10.1111/j.1471-4159.1991.tb02112.x.
To determine the type and the relative amount of prostaglandins (PGs) synthesized by various neural tissues, homogenates of meninges, dorsal root ganglia (DRG) capsules, decapsulated DRG, and unsheathed sciatic nerves were incubated with [1-14C]arachidonic acid. Homogenates of cultured cells (meningeal cells, fibroblasts, and nonneuronal or neuronal DRG cells) were used to specify the cells producing particular PGs. The highest synthetic capacity was found in fibroblast-rich tissues (meninges and DRG capsules) and in cultures of meningeal cells or fibroblasts. Two major cyclooxygenase products were formed: [14C]PGE2 and an unusual 14C-labeled compound, Y. The accumulation of compound Y, corresponding probably to 15-hydroperoxy PGE2, was completely impaired by addition of exogenous GSH, which conversely enhanced the synthesis of [14C]PGE2 and promoted the formation of [14C]PGD2. In contrast, decapsulated DRG or unsheathed sciatic nerves displayed a 10-20 times lower capacity to synthesize PGs than fibroblast-rich tissues and produced mainly [14C]PGE2 and [14C]PGD2. In this case, [14C]PGE2 or [14C]PGD2 synthesis was neither enhanced nor promoted by addition of exogenous GSH. Neuron-enriched DRG cell cultures allowed us to specify that [14C]PGD2 is the major prostanoid produced by primary sensory neurons as compared with nonneuronal DRG cells. Because PGD2 synthesis in DRG and more specifically in DRG neurons does not depend on exogenous GSH and differs from PGD2 synthesis in fibroblast-rich tissues, it is concluded that at least two distinct enzymatic processes contribute to PGD2 formation in the nervous system.(ABSTRACT TRUNCATED AT 250 WORDS)
为了确定各种神经组织合成的前列腺素(PGs)的类型和相对含量,将脑膜、背根神经节(DRG)被膜、去被膜DRG和无髓鞘坐骨神经的匀浆与[1-14C]花生四烯酸一起孵育。培养细胞(脑膜细胞、成纤维细胞以及非神经元或神经元DRG细胞)的匀浆用于确定产生特定PGs的细胞。在富含成纤维细胞的组织(脑膜和DRG被膜)以及脑膜细胞或成纤维细胞培养物中发现了最高的合成能力。形成了两种主要的环氧化酶产物:[14C]PGE2和一种不寻常的14C标记化合物Y。化合物Y的积累可能对应于15-氢过氧PGE2,添加外源性谷胱甘肽(GSH)可使其完全受损,相反,这会增强[14C]PGE2的合成并促进[14C]PGD2的形成。相比之下,去被膜DRG或无髓鞘坐骨神经合成PGs的能力比富含成纤维细胞的组织低10 - 20倍,并且主要产生[14C]PGE2和[14C]PGD2。在这种情况下,添加外源性GSH既不会增强也不会促进[14C]PGE2或[14C]PGD2的合成。富含神经元的DRG细胞培养物使我们能够确定,与非神经元DRG细胞相比,[14C]PGD2是初级感觉神经元产生的主要类前列腺素。由于DRG中,更具体地说是DRG神经元中的PGD2合成不依赖于外源性GSH,并且与富含成纤维细胞组织中的PGD2合成不同,因此得出结论,至少有两个不同的酶促过程参与神经系统中PGD2的形成。(摘要截短于250字)